Volume 2 Issue 4
Aug.  2012
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Mei Yang, Xin-Jun Xu, Chun-Yan Xie, Jie-Yun Huang, Zhi-Sheng Xie, De-Po Yang. Preparative isolation and purification of 12,13-dihydroxyeuparin from Radix Eupatorii Chinensis by high-speed counter-current chromatography[J]. Journal of Pharmaceutical Analysis, 2012, 02(4): 258-263. doi: 10.1016/j.jpha.2012.03.004
Citation: Mei Yang, Xin-Jun Xu, Chun-Yan Xie, Jie-Yun Huang, Zhi-Sheng Xie, De-Po Yang. Preparative isolation and purification of 12,13-dihydroxyeuparin from Radix Eupatorii Chinensis by high-speed counter-current chromatography[J]. Journal of Pharmaceutical Analysis, 2012, 02(4): 258-263. doi: 10.1016/j.jpha.2012.03.004

Preparative isolation and purification of 12,13-dihydroxyeuparin from Radix Eupatorii Chinensis by high-speed counter-current chromatography

doi: 10.1016/j.jpha.2012.03.004
Funds:

This work was supported by the International Scientific and Technological Cooperation Program of China

the Industry-University-Research Cooperation Program from Science and Technology Department of Guangdong Province

  • Publish Date: Aug. 10, 2012
  • An efficient method for the isolation and purification of 12,13-dihydroxyeuparin from Radix Eupatorii Chinensis by high speed counter-current chromatography (HSCCC) was established in this paper.The ether extracts of Radix Eupatorii Chinensis were purified by HSCCC with a solvent system of hexyl hydride ethyl acetate-methanol-water (1∶2∶1∶2,v/v/v/v).The upper phase was used as the stationary phase and the lower phase as the mobile phase.About 8.4 mg of 12,13-dihydroxyeuparin was obtained from 200 mg of ether extracts from Radix Eupatorii Chinensis in one-step HSCCC separation,with the purity of 96.71%,as determined by HPLC.After methanolwater recrystallization,the purity of 12,13-dihydroxyeuparin reached 99.83%.Such a simple and effective method was fairly useful to prepare pure compound as reference substances for related study on Radix Eupatorii Chinensis.
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